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N-PROPYL FORMATE-D1 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61219-61-2

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61219-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61219-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,1 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61219-61:
(7*6)+(6*1)+(5*2)+(4*1)+(3*9)+(2*6)+(1*1)=102
102 % 10 = 2
So 61219-61-2 is a valid CAS Registry Number.

61219-61-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-PROPYL FORMATE-D1

1.2 Other means of identification

Product number -
Other names Monodeuterio-ameisensaeure-propylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:61219-61-2 SDS

61219-61-2Upstream product

61219-61-2Downstream Products

61219-61-2Relevant academic research and scientific papers

KINETIC ISOTOPE EFFECT IN THE OXIDATION OF CYCLIC AND LINEAR ACETALS WITH OZONE AND MOLECULAR OXYGEN

Kuramshin, E. M.,Sadaeva, R. Kh.,Gumerova, V. K.,Zlot-skii, S. S.,Rakhmankulov, D. L.

, p. 136 - 139 (2007/10/02)

Substitution of hydrogen atoms at the acetal carbon by deuterium in 1,3-dioxolane, 1,3-dioxane, and dipropoxymethane leads to a decrease in the rate constant of ozonization and oxidation.The magnitude of the kinetic isotope effect lies in the range of 2-3 and is somewhat lower than the known values (4-6) for alcohols, ethers, and carboxylic acids.This is evidently due to the smaller extension of the C-H bond in the transition state of the reaction of acetals with ozone molecules and peroxide radicals.

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